RSS-Feed abonnieren
DOI: 10.1055/s-2005-837770
Olanzapine-Induced Acute Rhabdomyolysis
A Case ReportPublikationsverlauf
Received: 6.8.2003
Revised: 9.12.2003
Accepted: 10.12.2003
Publikationsdatum:
11. Februar 2005 (online)
Introduction
Olanzapine, a thienobenzodiazepine derivate, is a second-generation (atypical) antipsychotic agent with serotonin-dopamine-receptor-antagonism [2]. It has been shown in numerous clinical trials as equally effective in treating positive symptoms of schizophrenia, and more effective for negative and depressive symptoms than conventional antipsychotics. Most common adverse effects, which are relevant for patient-reported noncompliance in general [7], are weight gain and somnolence. In recent years uncommon side effects of olanzapine are reported more frequently [4]. Neuroleptic malignant syndrom (NMS) [5] [6] [15] or marked reversible elevation of serum creatine kinase (CK) associated with rhabdomyolysis [10] [13] is rare. We report a case of rhabdomyolysis with massive increase in CK activity after initiation of olanzapine monotherapy.
References
- 1 Allison R C, Bedsole D L. The other medical causes of rhabdomyolysis. Am J Med Sci. 2003; 326 79-88
- 2 Bhana N, Foster R H, Olney R, Plosker G L. Olanzapine: an updated review of its use in the management of schizophrenia. Drugs. 2001; 61 111-116
- 3 Beasley C M, Tollefson G D, Tran P V. Safety of olanzapine. J Clin Psychiatry. 1997; 58 (Suppl 10) 13-17
- 4 Farooque R. Uncommon side effects associated with olanzapine. Pharmacopsychiatry. 2003; 36 83
- 5 Johnson V, Bruxner G. Neuroleptic malignant syndrome associated with olanzapine. Aust N Z J Psychiatry. 1998; 32 884-886
- 6 Kopf A, Köster J, Schulz A, Krömker H, Becker T. Life threatening neuroleptic malignant syndrome due to olanzapine. Psychiatr Prax. 2003; 30 279-282
- 7 Löffler W, Kilian R, Toumi M, Angermeyer M C. Schizophrenic patients’ subjective reasons for compliance and noncompliance with neuroleptic treatment. Pharmacopsychiatry. 2003; 36 105-112
- 8 Marcus E L, Vass A, Zislin J. Marked elevation of serum creatine kinase associated with olanzapine therapy. Ann Pharmacother. 1999; 33 697-700
- 9 Meltzer H Y. Skeletal muscle necrosis following membrane-active drugs plus serotonin. J Neurol Sci. 1976; 28 41-56
- 10 Meltzer H Y, Cola P A, Parsa M. Marked elevation of serum creatine kinase activity associated with antipsychotic drug treatment. Neuropsychopharmacology. 1996; 15 395-405
- 11 Moretti-Rojas I, Ezrailson E G, Birnbaumer L, Entman M L, Garber A J. Serotonergic and adrenergic regulation of skeletal muscle metabolism in the rat. II. The use of 125iodolysergic acid diethylamide and 125iodopindolol as probes of sarcolemmal receptor function and specificity. J Biol Chem. 1983; 258 12 499-12 508
- 12 Poels P JE, Gabreels F JM. Rhabdomyolysis: a review of the literature. Clin Neurol Neurosurg. 1993; 95 175-192
- 13 Rosebraugh C J, Flockhart D A, Yasuda S U, Woosley R L. Olanzapine-induced rhabdomyolysis. Ann Pharmocother. 2001; 35 1020-1023
- 14 Shuster J. Olanzapine and rhabdomyolysis. Nursing. 2000; 30 87
- 15 Stanfield S C, Privette T. Neuroleptic malignant syndrome associated with olanzapine therapy: a case report. J Emerg Med. 2000; 19 355-357
- 16 Vanholder R, Mehmet S, Ekrem E, Lamiere N. Rhabdomyolysis. J Am Soc Nephrol. 2000; 11 1553-1561
-
17 http://www.akdae.de.20/20/Archiv/2002/20 020 315.html
Hermann Spießl, M.D.
Bezirksklinikum Regensburg
93042 Regensburg
Germany
Telefon: +49 941 941 1604
Fax: +49 941 941 1605
eMail: hermann.spiessl@bkr-regensburg.de